Senior clinical research coordinator vs clinical research coordinator

Differences between senior clinical research coordinator and clinical research coordinator duties and responsibilities

Senior clinical research coordinator example responsibilities.

• Work closely with investigators in identifying and managing adverse events and report events according to FDA requirements.
• Mentore and train employees on proper ICH and GCP clinical study procedures.
• Leverage exceptional working knowledge of good clinical practice (GCP) and ICH regulatory instructions during the execution of clinical trials.
• Co-Authore informed consents and consent patients while conducting information sessions with potential study subjects.
• Authore study specific documents according to FDA regulations.
• Conduct internal audits of oncology therapeutic trials for quality assurance purposes.
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Clinical research coordinator example responsibilities.

• Assess study participants for adverse reactions or complications and manage side effects of chemotherapy and other study relate drugs.
• Establish and maintain strong community partnerships to achieve HIV prevention objectives.
• Direct acquisition and analysis of functional MRI research data following GCP and FDA regulations
• Prepare and maintain IRB and regulatory documentation for various research projects and consent patients for clinical research.
• Facilitate constant communication between principal investigators, oncology nurses, and patients to address concerns and maximize eligibility and enrollment.
• Schedule patient for study procedures; initiate/coordinate drug orders, laboratory procedures and treatments for patients base on standing protocol orders.
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